29 quality engineer opportunities in Cambridge updated today
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· Page 1 / 2Job Description: The Design Quality Engineer (DQE) at Philips is responsible for ensuring that products are designed and developed in compliance with regulatory standards, quality requirements, and customer expectations. This role works closely with R&D, regulatory, manufacturing, and suppliers
Job Description: We are looking for an experienced CAPA Quality Engineer to drive CAPA initiatives, support project management activities, and communicate effectively across teams. The ideal candidate brings a minimum of five years of relevant experience and can quickly add value from day one. Respo
Job Description: The Design Quality Engineer (DQE) at Philips is responsible for ensuring that products are designed and developed in compliance with regulatory standards, quality requirements, and customer expectations. This role works closely with R&D, regulatory, manufacturing, and suppliers
Job Description: The Product Design Quality Engineer is responsible for supporting quality throughout the product development lifecycle by ensuring compliance with regulatory requirements, quality standards, and design control processes. This role partners with cross-functional teams to integrate qu
Job Description: Responsible for ensuring product quality, regulatory compliance, and process adherence in manufacturing environments by monitoring production activities, managing quality systems, and driving resolution of non-conformances. The role involves CAPA management, root cause analysis, aud
Job Description: Responsible for ensuring compliance to design controls, risk management, and verification/validation activities across the product lifecycle for medical devices, with a strong preference for ultrasound/imaging systems. Skill Requirement: Strong understanding of: Design controls &
Summary: The Quality Engineering Project Manager provides leadership, direction, and technical oversight for the Quality Engineering team within Operations. This role leads quality engineers who support manufacturing processes and provide quality engineering expertise for product, process, equipment
Description: Hybrid.. location can be Murrysville or Cambridge Job Title: CAPA Quality Engineer Job Responsibilities: Facilitate product and process Corrective and Preventive Action (CAPA) investigations from issue identification through implementation of solution and effectiveness monitoring. Pro
Job Title : Principal Device Quality Engineer - IVD devices SME ( JP9691) Location: Thousand Oaks, California OR San Francisco, California OR Cambridge, Massachusetts Employment Type : Contract Business Unit: Digital Health & Diagnostics Quality Duration : 12 months with likely extensions Job po
Job Title : Principal Device Quality Engineer - IVD devices SME ( JP9691) Location: Thousand Oaks, California OR San Francisco, California OR Cambridge, Massachusetts Employment Type : Contract Business Unit: Digital Health & Diagnostics Quality Duration : 12 months with likely extensions Job po
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful and usable solutions. From military defense and space exploration to biomedical e
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful and usable solutions. From military defense and space exploration to biomedical e
Design Verification Engineer Duration: 5 Months Location: Cambridge, MA, 02141 Job Description This position is responsible for the design, development, documentation and execution of all design verification plans, schedules, test protocols and reports to ensure the Measurement Sensors Platform at C
About Portal Instruments Portal Instruments is redefining how advanced injectable therapies are delivered. Founded on MIT research, Portal develops innovative drug-delivery platforms that enable patients to self-administer complex biologics safely, comfortably, and reliably. Our lead platform, PRIME
SanofiJob Title : Senior Quality Engineer, In Vitro Diagnostics Location: Cambridge, MA About the Job The Senior Quality Engineer – In Vitro Diagnostics is a senior subject matter expert responsible for ensuring the quality, safety, and regulatory compliance of IVD’s across the full product lifecycle—from
Job Title Software Design Quality Engineer Job Description The Software Design Quality Engineer is responsible for developing, maintaining, and managing comprehensive software quality documentation, ensuring their accuracy and regulatory compliance throughout the software lifecycle. Your role: Leads
Description: Hybrid.. location can be Murrysville or Cambridge Job Title: CAPA Quality Engineer Job Responsibilities: Facilitate product and process Corrective and Preventive Action (CAPA) investigations from issue identification through implementation of solution and effectiveness monitoring. • Pro
Summary: The Quality Engineering Project Manager provides leadership, direction, and technical oversight for the Quality Engineering team within Operations. This role leads quality engineers who support manufacturing processes and provide quality engineering expertise for product, process, equipment
Job Description: We are looking for an experienced CAPA Quality Engineer to drive CAPA initiatives, support project management activities, and communicate effectively across teams. The ideal candidate brings a minimum of five years of relevant experience and can quickly add value from day one. Respo
Relocation Assistance Offered Within Country Job Number #170882 - Cambridge, Ohio, United States Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products
Job Summary: We are seeking an experienced Supply Chain Program Manager / Supplier Quality Engineer to lead global supply chain initiatives supporting new product introductions (NPI), supplier transfers, sourcing programs, and supply chain readiness activities within a regulated manufacturing enviro
Job Summary: The Senior Design Quality Engineer will support product lifecycle management activities for medical devices by providing quality engineering leadership for design and process changes, risk management, verification and validation activities, and compliance with medical device regulations
In this exciting role as a Senior Quality Engineer, you will have responsibility for providing comprehensive manufacturing quality support for commercial medical devices in the area of component manufacturing. This includes activities related to test method validation, process validation, inspection
Quality Engineer Location: Woburn, MA (On-site) Reports To: Engineering Manager About Xico Lighting Xico Lighting is a rapidly growing manufacturer of spec-grade architectural lighting, driven by precision, performance, and design excellence. As we expand our in-house manufacturing and engineering c
Mondo Staffing AgencyJob Title: Senior Software Design Quality Engineer Start Date: ASAP Salary Range: $110,000 - $160,000/year Travel: Onsite 3 days per week in Danvers, MA Benefits: Eligible for Health, Dental, Vision, 401K, PTO Must be authorized to work in the U.S. This position is not eligible for sponsorship . The
Thank you for your interest in positions at IPG Photonics. All applicants must apply on our company website to be considered. Please visit www.ipgphotonics.com and click on the “Company” tab. We look forward to seeing your application soon! Job Summary: The Post Market Surveillance Quality Engineer
Job Summary: We are looking for an experienced Supplier Quality Engineer with 6–8 years of experience in supply chain, operations, engineering, or quality management within regulated industries such as Medical Devices, Pharmaceuticals, or Life Sciences. The candidate should have experience managing
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva , one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’l
This is a onsite position. The purpose of this position is to initiate medical device quality assurance activities. These activities must be in accordance with FDA Quality System Regulation, ISO13485 and other international standards. This position will also support device complaint investigation an
$29,000 – $47,000/year
Estimation confidence: Low
Estimate based on market data for Cambridge. Actual salaries may vary depending on experience, company, and area.
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